BEUDAMED
    FDA Adverse Event Other Summary report: N

    KARL STORZ

    MDR report key: 3109721 · Received May 3, 2013

    Report

    Report Number
    1221826-2013-00018
    Event Type
    Other
    Date Received
    May 3, 2013
    Manufacturer
    KARL STORZ ENDOVISION, INC.
    Product Code
    EOB
    PMA / PMN Number
    K072387
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THE VIDEO LARYNGOSCOPE WAS EVALUATED AND NO PROBLEM WAS FOUND. THE INVESTIGATION OF THIS ALLEGED ISSUE IS CURRENTLY TAKING PLACE AND WILL BE AVAILABLE AT A LATER DATE.

    Description of Event or Problem · 1

    IMP REF #(B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    195568 KARL STORZ VIDEO RHINO LARYNGOSCOPE EOB KARL STORZ ENDOVISION, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1